• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

采用间接竞争酶联免疫吸附测定法研究葛根素在大鼠体内的药代动力学和组织分布动力学

Pharmacokinetics and Tissue Distribution Kinetics of Puerarin in Rats Using Indirect Competitive ELISA.

作者信息

Kong Hui, Wang Xueqian, Shi Rongfeng, Zhao Yan, Cheng Jinjun, Yan Xin, Liu Xiaoman, Wang Yongzhi, Zhang Meiling, Wang Qingguo, Qu Huihua

机构信息

School of Chinese Medicine, Beijing Key Laboratory, Beijing University of Chinese Medicine, Beijing 100029, China.

School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 100029, China.

出版信息

Molecules. 2017 Jun 5;22(6):939. doi: 10.3390/molecules22060939.

DOI:10.3390/molecules22060939
PMID:28587251
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6152676/
Abstract

Puerarin (PUE) is a compound isolated from the roots of . We studied the pharmacokinetics and tissue distribution kinetics of PUE in Sprague-Dawley rats following intraperitoneal administration of three concentrations. Indirect competitive ELISA based on an anti-PUE monoclonal antibody was used to determine the concentration of PUE in the blood, heart, liver, spleen, lung, kidney, hippocampus, cerebral cortex, and striatum. The plasma and tissue distribution kinetic characteristics following a single injection of PUE (20, 40 and 80 mg/kg) were calculated using a non-compartment model. In the high-dose (80 mg/kg) and medium-dose (40 mg/kg) groups, the kinetic profile of PUE in blood and kidney samples showed two absorption peaks, while that of the other tissues showed only one peak. In the low-dose (20 mg/kg) group, there was only one peak, irrespective of the sample type. Pharmacokinetic parameters, such as the area under the curve, C, and T varied according to the administered dose. AUC and C values increased dose-dependently. PUE was widely distributed in areas of the brain such as the hippocampus, cerebral cortex, and striatum, providing a foundation for guiding the use of PUE in the treatment of cerebral ischaemic stroke and neurodegenerative diseases.

摘要

葛根素(PUE)是从[植物名称]根中分离出的一种化合物。我们研究了腹腔注射三种浓度的PUE后,其在Sprague-Dawley大鼠体内的药代动力学和组织分布动力学。基于抗PUE单克隆抗体的间接竞争ELISA法用于测定血液、心脏、肝脏、脾脏、肺脏、肾脏、海马体、大脑皮层和纹状体中PUE的浓度。采用非房室模型计算单次注射PUE(20、40和80 mg/kg)后的血浆和组织分布动力学特征。在高剂量(80 mg/kg)和中剂量(40 mg/kg)组中,血液和肾脏样本中PUE的动力学曲线显示有两个吸收峰,而其他组织仅显示一个峰。在低剂量(20 mg/kg)组中,无论样本类型如何,均只有一个峰。药代动力学参数,如曲线下面积、C和T,随给药剂量而变化。AUC和C值呈剂量依赖性增加。PUE广泛分布于大脑的海马体、大脑皮层和纹状体等区域,为指导PUE用于治疗脑缺血性中风和神经退行性疾病奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5ac/6152676/b0886cc0effd/molecules-22-00939-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5ac/6152676/bf171992cbb9/molecules-22-00939-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5ac/6152676/b0886cc0effd/molecules-22-00939-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5ac/6152676/bf171992cbb9/molecules-22-00939-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5ac/6152676/b0886cc0effd/molecules-22-00939-g002.jpg

相似文献

1
Pharmacokinetics and Tissue Distribution Kinetics of Puerarin in Rats Using Indirect Competitive ELISA.采用间接竞争酶联免疫吸附测定法研究葛根素在大鼠体内的药代动力学和组织分布动力学
Molecules. 2017 Jun 5;22(6):939. doi: 10.3390/molecules22060939.
2
Distribution kinetics of puerarin in rat hippocampus after acute local cerebral ischemia.葛根素在急性局部脑缺血后在大鼠海马中的分布动力学。
J Pharm Biomed Anal. 2019 Feb 5;164:196-201. doi: 10.1016/j.jpba.2018.10.038. Epub 2018 Oct 25.
3
Pharmacokinetics, tissue distribution and relative bioavailability of puerarin solid lipid nanoparticles following oral administration.葛根素固体脂质纳米粒经口服给药后的药代动力学、组织分布及相对生物利用度。
Int J Pharm. 2011 May 30;410(1-2):138-44. doi: 10.1016/j.ijpharm.2011.02.064. Epub 2011 Mar 15.
4
Effect of Puerarin on the Pharmacokinetics of Baicalin in Gegen Qinlian Decoction () in Mice.葛根素对小鼠葛根芩连汤中黄芩苷药代动力学的影响。
Chin J Integr Med. 2018 Jul;24(7):525-530. doi: 10.1007/s11655-015-1973-0. Epub 2015 Apr 24.
5
Pharmacokinetic, tissue distribution, and excretion of puerarin and puerarin-phospholipid complex in rats.葛根素及葛根素-磷脂复合物在大鼠体内的药代动力学、组织分布和排泄
Drug Dev Ind Pharm. 2006 Apr;32(4):413-22. doi: 10.1080/03639040600559123.
6
Puerarin-loaded PEG-PE micelles with enhanced anti-apoptotic effect and better pharmacokinetic profile.载葛根素的 PEG-PE 胶束,具有增强的抗凋亡作用和更好的药代动力学特征。
Drug Deliv. 2018 Nov;25(1):827-837. doi: 10.1080/10717544.2018.1455763.
7
[Effect of phenformin hydrochloride on pharmacokinetics of puerarin in rats].盐酸苯乙双胍对大鼠葛根素药代动力学的影响
Zhongguo Zhong Yao Za Zhi. 2012 Oct;37(19):2960-3.
8
Formulation optimization and bioavailability after oral and nasal administration in rabbits of puerarin-loaded microemulsion.葛根素微乳经口服和鼻腔给药后在兔体内的制剂优化和生物利用度。
J Pharm Sci. 2011 Mar;100(3):933-41. doi: 10.1002/jps.22333. Epub 2010 Sep 22.
9
A New Highly Selective and Specific Anti-puerarin polyclonal Antibody for Determination of Puerarin Using a Mannich Reaction Hapten Conjugate.一种用于通过曼尼希反应半抗原共轭物测定葛根素的新型高选择性和特异性抗葛根素多克隆抗体。
Pharmacogn Mag. 2018 Jan;13(Suppl 4):S845-S851. doi: 10.4103/pm.pm_276_17. Epub 2018 Jan 31.
10
RGD modified and PEGylated lipid nanoparticles loaded with puerarin: Formulation, characterization and protective effects on acute myocardial ischemia model.载葛根素的 RGD 修饰和聚乙二醇化脂质纳米粒:制剂、表征及对急性心肌缺血模型的保护作用。
Biomed Pharmacother. 2017 May;89:297-304. doi: 10.1016/j.biopha.2017.02.029. Epub 2017 Feb 24.

引用本文的文献

1
Studying targeted oxidation in diabetic cognitive dysfunction based on scientometrics analysis: research progress of natural product approaches.基于科学计量学分析的糖尿病认知功能障碍靶向氧化研究:天然产物方法的研究进展
Front Endocrinol (Lausanne). 2024 Dec 20;15:1445750. doi: 10.3389/fendo.2024.1445750. eCollection 2024.
2
Puerarin: a hepatoprotective drug from bench to bedside.葛根素:一种从实验室到临床的保肝药物。
Chin Med. 2024 Oct 8;19(1):139. doi: 10.1186/s13020-024-01011-y.
3
Enhanced Bioaccessibility of Microencapsulated Puerarin Delivered by Pickering Emulsions Stabilized with OSA-Modified Hydrolyzed Starch: In Vitro Release, Storage Stability, and Physicochemical Properties.

本文引用的文献

1
An assessment of the central disposition of intranasally administered insulin lispro in the cerebrospinal fluid of healthy volunteers and beagle dogs.健康志愿者和比格犬脑脊液中鼻内给予赖脯胰岛素的中枢处置评估。
Drug Deliv Transl Res. 2017 Feb;7(1):11-15. doi: 10.1007/s13346-016-0325-8.
2
Puerarin, isolated from Pueraria lobata (Willd.), protects against diabetic nephropathy by attenuating oxidative stress.从野葛(Pueraria lobata (Willd.))中分离出的葛根素通过减轻氧化应激来预防糖尿病肾病。
Gene. 2016 Oct 15;591(2):411-6. doi: 10.1016/j.gene.2016.06.032. Epub 2016 Jun 16.
3
Development and validation of an enzyme-linked immunosorbent assay for the quantification of gelonin in mouse plasma.
用经辛烯基琥珀酸酐(OSA)改性的水解淀粉稳定的皮克林乳液递送的微囊化葛根素的生物可及性增强:体外释放、储存稳定性及理化性质
Foods. 2022 Nov 11;11(22):3591. doi: 10.3390/foods11223591.
4
Protective effects and mechanism of puerarin targeting PI3K/Akt signal pathway on neurological diseases.葛根素靶向PI3K/Akt信号通路对神经疾病的保护作用及机制
Front Pharmacol. 2022 Oct 24;13:1022053. doi: 10.3389/fphar.2022.1022053. eCollection 2022.
5
Targeting Oxidative Stress in Intracerebral Hemorrhage: Prospects of the Natural Products Approach.靶向脑出血中的氧化应激:天然产物方法的前景
Antioxidants (Basel). 2022 Sep 14;11(9):1811. doi: 10.3390/antiox11091811.
6
Puerarin Attenuates Oxidative Stress and Ferroptosis via AMPK/PGC1α/Nrf2 Pathway after Subarachnoid Hemorrhage in Rats.葛根素通过AMPK/PGC1α/Nrf2通路减轻大鼠蛛网膜下腔出血后的氧化应激和铁死亡
Antioxidants (Basel). 2022 Jun 27;11(7):1259. doi: 10.3390/antiox11071259.
7
Puerarin Attenuates Cadmium-Induced Neuronal Injury via Stimulating Cadmium Excretion, Inhibiting Oxidative Stress and Apoptosis.葛根素通过刺激镉排泄、抑制氧化应激和细胞凋亡减轻镉诱导的神经元损伤。
Biomolecules. 2021 Jul 2;11(7):978. doi: 10.3390/biom11070978.
8
Puerarin attenuates intracerebral hemorrhage-induced early brain injury possibly by PI3K/Akt signal activation-mediated suppression of NF-κB pathway.葛根素通过激活 PI3K/Akt 信号通路抑制 NF-κB 通路减轻脑出血后早期脑损伤。
J Cell Mol Med. 2021 Aug;25(16):7809-7824. doi: 10.1111/jcmm.16679. Epub 2021 Jun 27.
9
Puerarin blocks the aging phenotype in human dermal fibroblasts.葛根素阻止人真皮成纤维细胞的衰老表型。
PLoS One. 2021 Apr 22;16(4):e0249367. doi: 10.1371/journal.pone.0249367. eCollection 2021.
10
Pharmacokinetics and drug delivery systems for puerarin, a bioactive flavone from traditional Chinese medicine.葛根素的药代动力学和药物传递系统,葛根素是一种来自中药的生物活性黄酮。
Drug Deliv. 2019 Dec;26(1):860-869. doi: 10.1080/10717544.2019.1660732.
用于定量小鼠血浆中相思子毒素的酶联免疫吸附测定法的开发与验证。
J Immunoassay Immunochem. 2016;37(6):611-22. doi: 10.1080/15321819.2016.1182551.
4
LC-MS/MS Analysis and Pharmacokinetics of Sodium (±)-5-Bromo-2-(α-hydroxypentyl) Benzoate (BZP), an Innovative Potent Anti-Ischemic Stroke Agent in Rats.(±)-5-溴-2-(α-羟基戊基)苯甲酸钠(BZP)的LC-MS/MS分析及其在大鼠体内的药代动力学研究,BZP是一种新型强效抗缺血性中风药物。
Molecules. 2016 Apr 16;21(4):501. doi: 10.3390/molecules21040501.
5
Protective Effect of Puerarin Against Oxidative Stress Injury of Neural Cells and Related Mechanisms.葛根素对神经细胞氧化应激损伤的保护作用及相关机制
Med Sci Monit. 2016 Apr 14;22:1244-9. doi: 10.12659/msm.896058.
6
Puerarin and betahistine treatment of vertebrobasilar ischemia vertigo: A meta-analysis of randomized controlled trials.葛根素与倍他司汀治疗椎基底动脉缺血性眩晕:一项随机对照试验的荟萃分析。
Exp Ther Med. 2016 Mar;11(3):1051-1058. doi: 10.3892/etm.2016.3004. Epub 2016 Jan 18.
7
Puerarin reduces apoptosis in rat hippocampal neurons culturea in high glucose medium by modulating the p38 mitogen activated protein kinase and c-Jun N-terminal kinase signaling pathways.葛根素通过调节p38丝裂原活化蛋白激酶和c-Jun氨基末端激酶信号通路,减少高糖培养基中大鼠海马神经元培养物中的细胞凋亡。
J Tradit Chin Med. 2016 Feb;36(1):78-84. doi: 10.1016/s0254-6272(16)30012-7.
8
Puerarin attenuates the inflammatory response and apoptosis in LPS-stimulated cardiomyocytes.葛根素减轻脂多糖刺激的心肌细胞中的炎症反应和细胞凋亡。
Exp Ther Med. 2016 Feb;11(2):415-420. doi: 10.3892/etm.2015.2910. Epub 2015 Dec 4.
9
Puerarin for ischaemic stroke.葛根素用于缺血性中风。
Cochrane Database Syst Rev. 2016 Feb 18;2:CD004955. doi: 10.1002/14651858.CD004955.pub3.
10
Puerarin Protects Pancreatic β-Cells in Obese Diabetic Mice via Activation of GLP-1R Signaling.葛根素通过激活GLP-1R信号通路保护肥胖糖尿病小鼠的胰岛β细胞。
Mol Endocrinol. 2016 Mar;30(3):361-71. doi: 10.1210/me.2015-1213. Epub 2016 Jan 20.